FDA 510(k)

矩陣數據管理系統

K 號：K162463 · 2017-05-24

決定日期2017-05-24

產品代碼DXN

諮詢委員會履歷

決定相當於

器材摘要

Matrix Data Management System is the device name listed in this FDA 510(k) record. The listed applicant is Global Instrumentation, LLC. It received FDA 510(k) clearance on 2017-05-24 under 510(k) number K162463. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Matrix Data Management System?

Matrix Data Management System is a medical device that received FDA 510(k) clearance on 2017-05-24. The listed applicant is Global Instrumentation, LLC. The 510(k) number is K162463.

When did Matrix Data Management System receive FDA 510(k) clearance?

Matrix Data Management System received FDA 510(k) clearance on 2017-05-24, under 510(k) number K162463.

Who is the listed applicant for Matrix Data Management System?

The FDA 510(k) record lists Global Instrumentation, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Matrix Data Management System?

The FDA product code for Matrix Data Management System is DXN.

其他以 Global Instrumentation, LLC 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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相關器械（代碼：DXN）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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